Bien-Air Dental SA
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
Devices registered here (1)
- Controller, Foot, Handpiece And CordProduct code EBW (opens in a new tab) · Class I · Dental · 21 CFR 872.4200
Recalls & enforcement
- Class IITerminated2015-08-27Possible loosening of the dental tool, which may lead to potential swallowing of the tool.
Related
- All facilities operated by BIEN-AIR DENTAL SA
- BIEN-AIR DENTAL SA (CH)
- Bien-Air Portugal Unipessoal LDA (PT)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Bien-Air Dental SA (FEI 3003268570) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003268570-bien-air-dental-sa/
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